FDA Inspection 1050614 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1047137

The FDA completed an inspection of CSL Plasma Inc. on Apr 20, 2018 in Louisville, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 20, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Louisville, KY (United States)